Synthesis of Novel Synthetic Vitamin K Analogues Prepared by

Feb 22, 2017 - Laboratory of Organic Synthesis and Medicinal Chemistry, Department of Bioscience and Engineering, College of Systems Engineering and S...
85 downloads 10 Views 954KB Size
Download PDF
This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

Brief Article pubs.acs.org/jmc

Synthesis of Novel Synthetic Vitamin K Analogues Prepared by Introduction of a Heteroatom and a Phenyl Group That Induce Highly Selective Neuronal Differentiation of Neuronal Progenitor Cells Kimito Kimura,† Yoshihisa Hirota,‡ Shigefumi Kuwahara,§ Atsuko Takeuchi,∥ Chisato Tode,∥ Akimori Wada,⊥ Naomi Osakabe,# and Yoshitomo Suhara*,† †

Laboratory of Organic Synthesis and Medicinal Chemistry, Department of Bioscience and Engineering, College of Systems Engineering and Science, Shibaura Institute of Technology, 307 Fukasaku, Minuma-ku, Saitama 337-8570, Japan ‡ Laboratory of Biochemistry, Department of Bioscience and Engineering, College of Systems Engineering and Science, Shibaura Institute of Technology, 307 Fukasaku, Minuma-ku, Saitama 337-8570, Japan § Laboratory of Applied Bioorganic Chemistry, Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai, 981-8555, Japan ∥ Analytical Laboratory, Kobe Pharmaceutical University, 4-19-1 Motoyamakita-machi, Higashinada-ku, Kobe 658-8558, Japan ⊥ Department of Life Science for Organic Chemistry, Kobe Pharmaceutical University, 4-19-1 Motoyamakita-machi, Higashinada-ku, Kobe 658-8558, Japan # Food and Nutrition Laboratory, Department of Bioscience and Engineering, College of Systems Engineering and Science, Shibaura Institute of Technology, 307 Fukasaku, Minuma-ku, Saitama 337-8570, Japan S Supporting Information *

ABSTRACT: We synthesized novel vitamin K2 analogues that incorporated a heteroatom and an aromatic ring in the side chain and evaluated their effect on the selective differentiation of neuronal progenitor cells into neurons in vitro. The results showed that a menaquinone-2 analogue bearing a p-fluoroaniline had the most potent activity, which was more than twice as great as the control. In addition, the neuronal selectivity was more than 3 times greater than the control.

■

brain tissues. We focused on “organic compounds” that promote NPCs differentiation and maturation for establishing safe and practical cell therapies. Several natural products have been identified that directly affected differentiation of NPCs into neurons, astrocytes, and oligodendrocytes; however, the compounds demonstrated no selectivity or only weak activity.4 We previously reported that menaquinone-4, one of the vitamin K homologues, was biosynthesized and was used in the brain.5 There are two natural forms of vitamin K homologues, plant-derived vitamin K1 (phylloquinone, PK) (1) and the bacterium-derived vitamin K2 (2) (menaquinone-n, MK-n) including MK-2 (3), MK-3 (4), and MK-4 (5) (Figure 1). In contrast, vitamin K3 (menadione) (6) is an artificial vitamin K. We have recently revealed that MK-4 had the selective ability to cause differentiation of NPCs, derived from mouse cerebrum,

INTRODUCTION Neural progenitor cells (NPCs) are located in several regions of the human adult brain such as the subventricular zone and the dentate gyrus of the hippocampus. NPCs can contribute to neurogenesis in adulthood because they are capable of differentiating into neurons, astrocytes, and oligodendrocytes.1 Therefore, NPCs would have possible applications for development of stem-cell-based therapies for neurodegenerative diseases.2 It have been reported that the grafting of NPCs improves neurological deficits in neurodegenerative diseases such as Parkinson’s disease, ischemic stroke, and spinal cord injury.3 However, the induction of new neuronal cells in the damaged brain is relatively low and might be nonfunctional. Otherwise, the transplantation of neural stem cells was expected to repair lesions, since they could differentiate into neurons. But transplanted cells also had difficulties of differentiation, maturation, and integration into host neural networks. We have explored a new strategy to repair damaged © 2017 American Chemical Society

Received: November 28, 2016 Published: February 22, 2017 2591

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596

Journal of Medicinal Chemistry

Brief Article

prepared by introducing a nitrogen atom or an oxygen atom as well as phenyl groups. At first, we planned the synthesis of the side chain by introduction of the nitrogen atom using aniline derivatives, followed by a coupling reaction with vitamin K3 by Friedel−Crafts alkylation. However, the coupling reaction did not proceed at all. Presumably, the nitrogen atom incorporated into the side chain interrupted the progress of the reaction with vitamin K3. Therefore, we reconsidered the order of the synthetic coupling reactions between the side chain and vitamin K3. We first synthesized vitamin K homologues 3 and 4 by a coupling reaction with geraniol (19) or farnesol (20) and a hydroquinone according to a previously reported method.8 After 6 was reduced to the hydroquinone derivative with a 10% sodium hydrosulfite (aq) solution in diethyl ether, the isoprene unit 19 or 20 was successively coupled with the hydroquinone in the presence of a catalytic amount of BF3·Et2O to give 3 and 4 in 34% and 32% yield, respectively. Then, the hydroxyl group was introduced to the carbon atom of ω-terminal side chain in 3 and 4 to give alcohols 21 and 22 in 30% and 5% yield, respectively. Since the side chain length of 4 was longer than that of 3, the selectivity of introduction of the oxygen at the ωposition of 4 did not proceed very well. The alcohols 21 and 22 were oxidized with MnO2 to obtain aldehydes 23 and 24 in 78% and 76% yield, respectively.9 Introduction of the nitrogen atom into the side chain of vitamin K was provided by reductive amination reaction between 23 or 24 and aniline derivatives. Incorporation of an oxygen atom in the side chain was successfully carried out with Mitsunobu reaction between 21 or 22 and phenol derivatives. Thus, the individual desired vitamin K analogues of aniline derivatives 7−9 and 13−15 were obtained in 52−78% yield. The phenol derivatives 10−12 and 16−18 were obtained in 43−82% yield. We investigated the differentiation-inducing activity of the vitamin K analogues using NPCs, which were prepared from embryonic mouse brain. The general method for preparation was as follows as we previously reported:7 (i) Neural stem cells were dissociated from embryonic day 14 mouse cerebrum and cultured according to the method previously described.10 (ii) After the cells were seeded and cultured for 24 h, they were treated with 1 μM vitamin K analogues every second day for 4 days. We confirmed the differentiation of the NPCs by an immunofluorescence staining method. The specific antigen microtubule-associated protein 2 (Map2) was expressed on the surface of neuronal cells that had successfully differentiated from progenitor cells, and the sample emitted red fluorescence. On the other hand, the expression of glial fibrillary acidic protein (Gfap), indicating differentiation to the astrocyte, was detected as green emission. The differentiation could be evaluated from the resulting fluorescence with fluorescence microscopy (Figure 2). In the ethanol control, we observed the differentiation of NPCs into only neuronal cells. On the other hand, natural menaquinone 5 promoted the differentiation of NPCs into neuronal cells and astrocytes. The analogues 9 (with a nitrogen substituent in the side chain) and 17 (with a phenol substituent) promoted the selective differentiation of NPCs into neuronal cells since the differentiated cells mostly exhibited red fluorescence but no green fluorescence. Then we quantitated the mRNA of Map2, Gfap, and β-actin of the cells using real-time PCR methodology to measure the differentiation activity (Figure 3). The samples treated with EtOH as untreated controls and with menaquinones 3−5 as positive controls were used for the purpose of comparison with our compounds. In Figure 3A, the data were derived from

Figure 1. Structure of vitamin K homologues: vitamin K1 (1), vitamin K2 (2) (MK-2 (3), MK-3 (4), MK-4 (5)), and vitamin K3 (6).

into neuronal cells. Vitamin K homologues also have been reported to play a role in preventing oxidative injury to developing oligodendrocytes and neurons.6 On the basis of these findings, we have synthesized new vitamin K analogues modified at the ω-terminal group, and several analogues with introduction of aromatic groups exhibited potent differentiation activity compared to natural vitamin K.7 The activity of the compound was double that of the control, and it was also neuronal selective. This finding showed modification of the side chain of vitamin K could increase the differentiation activity. However, much more potent activity is necessary for application as therapeutic agents. If the analogues exhibited strong differentiation activity in neuronal cells, they may be applicable to elucidate the mechanism of vitamin K in the brain. In this study, we synthesized new analogues by introduction of a heteroatom and an aromatic ring in the molecule with the expectation of interaction with target proteins related to differentiation. Here, we report the synthesis and structure− activity relationship of novel vitamin K2 analogues that selectively induced neuronal differentiation of multipotent neural progenitor cells.

■

RESULTS AND DISCUSSION The requisite vitamin K2 analogues containing aromatic rings and heteroatoms at the ω-terminal position were obtained by the synthetic method as shown in Scheme 1. Compounds were Scheme 1. Synthesis of Vitamin K Analogues 7−18a

Reagents and conditions: (a) 10% Na2S2O4 aq, Et2O, quant; (b) BF3· Et2O, 32−34%; (c) SeO2, salicylic acid, 70% TBHP, 5−30%; (d) MnO2, 76−78%; (e) aniline derivative, AcOH, NaBH(OAc)3, 52− 78%; (f) phenol derivative, Ph3P, DIAD, 43−82%. a

2592

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596

Journal of Medicinal Chemistry

Brief Article

activity as 5. There were no significant differences between 5 and 9 by Student’s t-test. While the activity of the MK-2 analogue 7 was significantly higher than that of the EtOH control. Among the phenol derivatives, 16 and 17 showed higher activity but with significantly lower effects than 7 and 9 (Figure 3A). On the other hand, Figure 3B was obtained from calculation of the mRNA level of Gfap/β-actin same as Figure 3A. This graph indicated that 5 significantly increased expression of the mRNA level of Map2 and Gfap, while 7, 9, 16, and 17 promoted only Map2. To evaluate selective differentiation activity of vitamin K analogues toward neuronal cells, we also calculated the relative ratio of the mRNA of Map2/Gfap from the data of Figure 3 as shown in Figure 4. From this result, 9 and 17 showed

Figure 2. Vitamin K derivatives induce neuronal differentiation of NPCs isolated from an embryonic mouse cerebrum. The cells were treated with the indicated compounds 5, 9, and 17 at 1 μM. After 48 h, cells were immunostained with markers for neurons (Map2, red) and astrocytes (Gfap, green) and also with DAPI (blue) for nuclei. Mature neurons and a very small amount of astrocytes were respectively observed with Map2 (red) and Gfap (green) after treatment with MK4 (5), a natural menaquinone. On the other hand, the synthesized analogues 9 (bearing a nitrogen) and 17 (bearing a phenol) induced only neuronal differentiation.

Figure 4. Relative ratios of differentiation-inducing activity of vitamin K2 analogues to convert neuronal progenitor cells into neuronal cells or astrocyte cells, as determined by calculation of the relative ratios of Map2/Gfap from the data of Figure 3. The data were normalized with respect to that obtained with the EtOH control, which was expressed as 1.0. Cells were treated with the indicated vitamin K2 analogues 7− 18 as well as natural menaquinones 3−5 and menadione 6 at 1.0 × 10−6 M. Compounds 7−12 were MK-2 analogues, and 13−18 were MK-3 analogues. The histogram data are expressed as mean values obtained from three independent experiments. The error bars indicate the SD. Significant differences: (∗∗∗) p < 0.001, (∗) p < 0.01, between EtOH and the compounds (by Dunnett’s t-test); (##) p < 0.005 between 5 and 9 (by Student’s t-test).

Figure 3. Differentiation-inducing activity of vitamin K2 analogues from neuronal progenitor cells into neuronal cells as determined by quantitation of mRNA synthesis for Map2 and β-actin (A), Gfap and β-actin (B) using PCR methodology. The relative ratios were calculated for Map2/β-actin (A) and Gfap/β-actin (B), respectively, and then the data were normalized with respect to the EtOH control, which was expressed as 1.0. Cells were treated with the indicated vitamin K2 analogues as well as natural menaquinones 3−5 and menadione 6 at 1.0 × 10−6 M. Compounds 7−12 were MK-2 analogues, and 13−18 were MK-3 analogues. The histogram data are expressed as the mean values obtained from three independent experiments; the error bars indicate the SD. Significant difference: (∗∗∗) p < 0.001, (∗∗) p < 0.005, (∗) p < 0.01, between EtOH and compounds (by Dunnett’s t-test). There are no significant differences between 5 and 9 (by Student’s t-test) in (A).

significantly higher ratios compared to control (EtOH). Thus, these compounds promoted selective differentiation into neuronal cells rather than into astrocyte cell. Overall, MK-2 analogues bearing an aniline group and MK-3 analogues possessing a phenol tended to exhibit highly selective differentiation activity toward neuronal cells. Specifically, 9 showed the highest effects for selectivity and activity among the compounds. The selectivity was much higher than that observed with natural vitamin K2. As compared to the natural menaquinone 5, 9 selectively favored the production of neuronal cells, as confirmed by Student’s t-test (Figure 4). The effects of the vitamin K on NPCs differentiation have not been investigated until now. Recently, it was reported that vitamin E isomer δ-tocopherol enhanced the efficiency of neural stem cell differentiation via the L-type calcium channel.11 The side chain part of δ-tocopherol and vitamin K resemble each other, suggesting that the mechanism of differentiation might also be mediated through a calcium channel.

calculation of the ratio of the mRNA levels of Map2/β-actin. The ratio obtained for the untreated control (EtOH) was expressed as 1.0, and the values for the analogues were expressed with respect to the control value. Most of the analogues effectively increased the expression of the mRNA level of Map2. This result suggests that most compounds enhanced the differentiation-inducing activity toward neuronal cells compared to controls. Among natural menaquinones, 5 showed the highest activity that was more than twice the response of the control in this experiment. Interestingly, the MK-2 analogue 9, modified with the p-fluoroaniline at the ωterminal position of 3, showed the most potent activity among the synthetic analogues. It was also more than 3 times as effective as the EtOH control and displayed almost the same

■

CONCLUSION We successfully introduced nitrogen or oxygen atoms into the side chain of vitamin K derivatives to produce new analogues. We found that some of these compounds had selective and potent activity toward the differential of neuronal progenitor cells into mature neuronal cells. We clarified that significant differences in differentiation activity could be obtained by 2593

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596

Journal of Medicinal Chemistry

Brief Article

MHz, CDCl3): δ 185.5, 184.6, 156.8, 154.5, 146.1, 144.9, 143.4, 137.2, 133.45, 133.40, 132.5, 132.20, 132.18, 126.4, 126.3, 125.9, 119.5, 115.6, 115.4, 113.7, 113.6, 52.4, 39.4, 26.2, 26.1, 16.5, 14.8, 12.8. HRMS ([M + H]+) m/z calcd for C27H29FNO2 418.2182; found 418.2182. 2-((2E,6E)-3,7-Dimethyl-8-phenoxyocta-2,6-dien-1-yl)-3methylnaphthalene-1,4-dione (10). To a solution of MK-2 ωalcohol 21 (24 mg, 110 μmol) in THF (2 mL) were added phenol (31 mg, 330 μmol) and triphenylphosphine (87 mg, 330 μmol) at 0 °C under argon. After stirring for 30 min at the same temperature, diisopropyl azodicarboxylate (67 mg, 330 μmol) in THF (1 mL) was added dropwise to the mixture. The reaction mixture was stirred for 1 h at room temperature, then diluted with ethyl acetate (50 mL). The mixture was washed with brine (50 mL), dried over MgSO4, and concentrated. The residue was purified with silica gel column chromatography (n-hexane/ethyl acetate = 30:1) to afford 10 (23 mg, 78%) as a yellow oil. 1H NMR (400 MHz, CDCl3); δ 8.09−8.06 (2H, m), 7.69−7.67 (2H, m), 7.26−7.22 (2H, m), 6.93−6.84 (3H, m), 5.49−5.45 (1H, m), 5.05−5.02 (1H, m), 4.31 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.19 (3H, s), 2.19−2.14 (2H, m), 2.06−2.02 (2H, m), 1.80 (3H, s), 1.70 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 159.0, 146.1, 143.5, 137.2, 133.45, 133.40, 132.22, 132.19, 131.3, 129.4, 128.4, 126.4, 126.3, 120.7, 119.6, 114.9, 73.9, 39.2, 26.2, 26.1, 16.5, 14.0, 12.8. HRMS ([M + H]+) m/z calcd for C27H29O3 401.2117; found 401.2114. 2-((2E,6E)-3,7-Dimethyl-8-(m-tolyloxy)octa-2,6-dien-1-yl)-3methylnaphthalene-1,4-dione (11). Similar to the synthesis of 10 from 21, the crude product 11, which was obtained from the reaction of a mixture of 21 (61 mg, 188 μmol), m-cresol (61 mg, 564 μmol), and triphenylphosphine (148 mg, 564 μmol) in THF (4 mL), and diisopropyl azodicarboxylate (114 mg, 564 μmol) in THF (2 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 40:1), giving 11 (60 mg, 77%) as a yellow oil. 1H NMR (400 MHz, CDCl3): δ 8.08−8.06 (2H, m), 7.69−7.65 (2H, m), 7.15−7.10 (1H, m), 6.76−6.65 (3H, m), 5.48−5.44 (1H, m), 5.05−5.02 (1H, m), 4.29 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.30 (3H, s), 2.19 (3H, s), 2.19−2.14 (2H, m), 2.06−2.02 (2H, m), 1.80 (3H, s), 1.70 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 159.0, 146.1, 143.5, 139.4, 137.2, 133.45, 133.40, 132.23, 132.21, 131.4, 129.1, 128.3, 126.4, 126.3, 121.5, 119.6, 115.8, 111.7, 73.9, 39.2, 26.3, 26.1, 21.6, 16.5, 14.0, 12.8. HRMS ([M + Na]+) m/z calcd for C28H30NaO3 437.2093; found 437.2092. 2-((2E,6E)-3,7-Dimethyl-8-(4-nitrophenoxy)octa-2,6-dien-1yl)-3-methylnaphthalene-1,4-dione (12). Similar to the synthesis of 10 from 21, the crude product 12, which was obtained from the mixture of 21 (39 mg, 120 μmol), p-nitrophenol (50 mg, 360 μmol), and triphenylphosphine (94 mg, 360 μmol) in THF (4 mL) and diisopropyl azodicarboxylate (73 mg, 360 μmol) in THF (1.5 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate= 10:1), giving 12 (44 mg, 82%) as a yellow oil. 1H NMR (400 MHz, CDCl3): δ 8.20−8.14 (2H, m), 8.08−8.05 (2H, m), 7.71−7.66 (2H, m), 6.92−6.88 (2H, m), 5.51−5.47 (1H, m), 5.05−5.02 (1H, m), 4.40 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.21−2.16 (2H, m), 2.19 (3H, s), 2.07−2.04 (2H, m), 1.81 (3H, s), 1.70 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 164.0, 146.1, 143.5, 141.4, 136.8, 133.5, 133.4, 132.2, 130.0, 129.6, 126.34, 126.31, 125.9, 119.9, 114.8, 74.6, 39.1, 26.1, 16.4, 13.9, 12.8. HRMS ([M + Na]+) m/z calcd for C27H27NNaO5 468.1787; found 468.1787. 2-Methyl-3-((2E,6E,10E)-3,7,11-trimethyl-12-(phenylamino)dodeca-2,6,10-trien-1-yl)naphthalene-1,4-dione (13). Similar to the synthesis of 7 from 23, the crude product 13, which was obtained from MK-3 ω-aldehyde 24 (53 mg, 136 μmol), aniline (14 μL, 150 μmol), acetic acid (10 μL, 150 μmol), MS4A, and sodium triacetoxyborohydride (50 mg, 236 μmol) in CH2Cl2 (2 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 13 (37 mg, 58%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 8.09−8.06 (2H, m), 7.69−7.67 (2H, m), 7.16−7.12 (2H, m), 6.68−6.58 (3H, m), 5.36−5.33 (1H, m), 5.02 (2H, dd, J = 7.2, 14.4 Hz), 3.77 (1H, br s), 3.60 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.18 (3H, s), 2.09−1.91 (8H, m), 1.79 (3H, s), 1.62 (3H, s), 1.55 (3H, s).

altering the functional group and the heteroatom of the side chain. A more detailed examination is underway to clarify the mechanism of action of these vitamin K analogues. If the mechanism and the target protein are clarified, it may be possible to design and synthesize much more potent compounds based on our findings.

■

EXPERIMENTAL SECTION

High-resolution ESI-MS (ESI-HRMS) was performed with a Micromass Q-TOF mass spectrometer. 1H NMR spectra were recorded at 400 MHz and 13C NMR spectra were recorded at 100 MHz using CDCl3 as a solvent unless otherwise specified. Chemical shifts are given in parts per million (δ) using tetramethylsilane (TMS) as the internal standard. Column chromatography was carried out on silica gel 60 (70−230 mesh). The nuclei were stained with DAPI. Cells were fixed with 10% formaldehyde solution, viewed under a fluorescent microscope, and photographed. Unless otherwise noted, all reagents were purchased from commercial suppliers. We confirmed that the purities of the 7−18 attained more than 95% as determined by HPLC (high pressure liquid chromatography). 2-((2E,6E)-3,7-Dimethyl-8-(phenylamino)octa-2,6-dien-1-yl)3-methylnaphthalene-1,4-dione (7). To a solution of MK-2 ωaldehyde 23 (51 mg, 158 μmol) in CH2Cl2 (2 mL) were added aniline (18 mg, 190 μmol) and acetic acid (11 mg, 190 μmol), and the mixture was stirred in the presence of molecular sieves 4A (MS4A) at room temperature for 30 min under argon. After the mixture was cooled to 0 °C, sodium triacetoxyborohydride (67 mg, 316 μmol) was added to the solution. The mixture was stirred at room temperature for 6 h, then diluted with ethyl acetate (50 mL). The solution was washed with 5% NaHCO3 aq (50 mL) and brine (50 mL), dried over MgSO4, and concentrated. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1) to afford 7 (36 mg, 57%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 8.09− 8.06 (2H, m), 7.69−7.67 (2H, m), 7.17−7.11 (2H, m), 6.69−6.54 (3H, m), 5.36−5.32 (1H, m), 5.03−4.99 (1H, m), 3.74 (1H, br s), 3.57 (2H, s), 3.36 (2H, d, J = 6.8 Hz), 2.18 (3H, s), 2.15−2.09 (2H, m), 2.05−1.99 (2H, m), 1.78 (3H, s), 1.63 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.6, 184.6, 148.6, 146.2, 143.5, 137.3, 133.5, 133.4, 132.6, 132.24, 132.22, 129.2, 126.4, 126.3, 125.8, 119.5, 117.2, 112.9, 51.8, 39.4, 26.3, 26.1, 16.5, 14.8, 12.8. HRMS ([M + H]+) m/z calcd for C27H30NO2 400.2277; found 400.2279. 2-((2E,6E)-3,7-Dimethyl-8-(p-tolylamino)octa-2,6-dien-1-yl)3-methylnaphthalene-1,4-dione (8). Similar to the synthesis of 7 from 23, the crude product 8, which was obtained from reaction of 23 (31 mg, 96 μmol), p-toluidine (12 mg, 115 μmol), acetic acid (7 μL, 115 μmol), MS4A, and sodium triacetoxyborohydride (41 mg, 192 μmol) in CH2Cl2 (2 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 8 (23 mg, 58%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 8.09−8.07 (2H, m), 7.69−7.67 (2H, m), 6.97−6.92 (2H, m), 6.55−6.48 (2H, m), 5.35−5.32 (1H, m), 5.02−4.99 (1H, m), 3.55 (2H, s), 3.36 (2H, d, J = 7.2 Hz), 2.21 (3H, s), 2.18 (3H, s), 2.14−2.09 (2H, m), 2.04−1.98 (2H, m), 1.78 (3H, s), 1.63 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 146.3, 146.2, 143.5, 137.3, 133.5, 133.4, 132.8, 132.2, 129.7, 126.4, 126.3, 125.7, 119.5, 113.1, 52.2, 39.5, 26.3, 26.1, 20.4, 16.5, 14.8, 12.8. HRMS ([M + H]+) m/z calcd for C28H32NO2 414.2433; found 414.2432. 2-((2E,6E)-8-((4-Fluorophenyl)amino)-3,7-dimethylocta-2,6dien-1-yl)-3-methylnaphthalene-1,4-dione (9). Similar to the synthesis of 7 from 23, the crude product 9, which was obtained from reaction of 23 (92 mg, 285 μmol), p-fluoroaniline (33 μL, 342 μmol), acetic acid (20 μL, 342 μmol), MS4A, and sodium triacetoxyborohydride (121 mg, 174 μmol) in CH2Cl2 (3 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 9 (93 mg, 78%) as a brown oil. 1H NMR (400 MHz, CDCl3); δ 8.07−8.05 (2H, m), 7.68−7.66 (2H, m), 6.88−6.79 (2H, m), 6.55− 6.46 (2H, m), 5.34−5.30 (1H, m), 5.02−4.99 (1H, m), 3.66 (1H, br s), 3.52 (2H, s), 3.35 (2H, d, J = 6.8 Hz), 2.17 (3H, s), 2.14−2.09 (2H, m), 2.02−1.99 (2H, m), 1.78 (3H, s), 1.62 (3H, s). 13C NMR (100 2594

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596

Journal of Medicinal Chemistry

Brief Article

C NMR (100 MHz, CDCl3); δ 185.6, 184.6, 148.6, 146.2, 143.4, 137.5, 134.9, 133.5, 133.4, 132.3, 132.23, 132.20, 129.2, 126.4, 126.3, 126.2, 124.2, 119.2, 117.2, 112.9, 51.9, 39.8, 39.4, 26.51, 26.45, 26.1, 16.5, 16.1, 14.8, 12.8. HRMS ([M + H]+) m/z calcd for C32H38NO2 468.2903; found 468.2906. 2-Methyl-3-((2E,6E,10E)-3,7,11-trimethyl-12-(p-tolylamino)dodeca-2,6,10-trien-1-yl)naphthalene-1,4-dione (14). Similar to the synthesis of 7 from 23, the crude product 14, which was obtained from 24 (45 mg, 115 μmol), p-toluidine (15 mg, 138 μmol), acetic acid (8 μL, 138 μmol), MS4A, and sodium triacetoxyborohydride (49 mg, 230 μmol) in CH2Cl2 (2 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 14 (38 mg, 68%) as a brown oil. 1H NMR (400 MHz, CDCl3); δ 8.09−8.06 (2H, m), 7.70−7.67 (2H, m), 6.95 (2H, d, J = 7.6 Hz), 6.53−6.50 (2H, m), 5.35−5.31 (1H, m), 5.05−4.99 (2H, m), 3.57 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.21 (3H, s), 2.18 (3H, s), 2.08−1.91 (8H, m), 1.80 (3H, s), 1.62 (3H, s), 1.55 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.6, 184.6, 146.4, 146.2, 143.4, 137.6, 135.0, 133.5, 133.4, 132.5, 132.24, 132.20, 129.7, 126.4, 126.3, 126.1, 124.2, 119.2, 113.0, 52.3, 39.8, 39.4, 26.52, 26.45, 26.1, 20.5, 16.5, 16.1, 14.8, 12.8. HRMS ([M + H]+) m/z calcd for C33H40NO2 482.3059; found 482.3057. 2-((2E,6E,10E)-12-((4-Fluorophenyl)amino)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)-3-methylnaphthalene-1,4-dione (15). Similar to the synthesis of 7 from 23, the crude product 15, which was obtained from 24 (54 mg, 138 μmol), p-fluoroaniline (16 μL, 166 μmol), acetic acid (10 μL, 166 μmol), MS4A, and sodium triacetoxyborohydride (59 mg, 276 μmol) in CH2Cl2 (2 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 15 (45 mg, 67%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 8.09−8.06 (2H, m), 7.69−7.66 (2H, m), 6.85 (2H, t, J = 8.4 Hz), 6.54−6.49 (2H, m), 5.33 (1H, t, J = 6.9 Hz), 5.04−4.99 (2H, m), 3.66 (1H, br s), 3.56 (2H, s), 3.37 (2H, d, J = 6.9 Hz), 2.18 (3H, s), 2.08−1.91 (8H, m), 1.79 (3H, s), 1.61 (3H, s), 1.55 (3H, s). 13C NMR (100 MHz, CDCl3); δ 185.6, 184.6, 156.8, 154.5, 146.2, 144.9, 143.4, 137.5, 134.9, 133.5, 133.4, 132.22, 132.19, 132.15, 126.4, 126.3, 124.2, 119.2, 115.7, 115.4, 113.7, 113.6, 52.5, 39.8, 39.4, 26.5, 26.4, 26.1, 16.5, 16.1, 14.7, 12.8. HRMS ([M + H]+) m/z calcd for C32H37FNO2 486.2756; found 486.2808. 2-Methyl-3-((2E,6E,10E)-3,7,11-trimethyl-12-phenoxydodeca-2,6,10-trien-1-yl)naphthalene-1,4-dione (16). Similar to the synthesis of 10 from 21, the crude product 16, which was obtained from the mixture of MK-3 ω-alcohol 22 (41 mg, 104 μmol), phenol (29 mg, 312 μmol), and triphenylphosphine (82 mg, 312 μmol) in THF (3 mL) and diisopropyl azodicarboxylate (63 mg, 312 μmol) in THF (1.5 mL), was purified by silica gel column chromatography (nhexane/ethyl acetate = 40:1), giving 16 (26 mg, 53%) as a yellow oil. 1 H NMR (400 MHz, CDCl3): δ 8.09−8.06 (2H, m), 7.69−7.67 (2H, m), 7.27−7.23 (2H, m), 6.93−6.89 (3H, m), 5.47 (1H, dd, J = 6.0, 6.8 Hz), 5.07−5.00 (2H, m), 4.35 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.18 (3H, s), 2.14−1.95 (8H, m), 1.79 (3H, s), 1.69 (3H, s), 1.57 (3H, s). 13 C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 159.1, 146.2, 143.4, 137.5, 134.8, 133.44, 133.38, 132.25, 132.22, 131.0, 129.4, 128.8, 126.4, 126.3, 124.3, 120.7, 119.2, 114.9, 74.0, 39.7, 39.2, 26.5, 26.4, 26.1, 16.5, 16.1, 14.0, 12.8. HRMS ([M + Na]+) m/z calcd for C32H36NaO3 491.2562; found 491.2562. 2-Methyl-3-((2E,6E,10E)-3,7,11-trimethyl-12-(m-tolyloxy)dodeca-2,6,10-trien-1-yl)naphthalene-1,4-dione (17). Similar to the synthesis of 10 from 21, the crude product 17, which was obtained from the mixture of 22 (59 mg, 150 μmol), m-cresol (49 mg, 450 μmol), and triphenylphosphine (118 mg, 450 μmol) in THF (5 mL) and diisopropyl azodicarboxylate (91 mg, 450 μmol) in THF (1 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 40:1), giving 17 (31 mg, 43%) as a yellow oil. 1H NMR (400 MHz, CDCl3): δ 8.09−8.06 (2H, m), 7.69−7.67 (2H, m), 7.15−7.11 (1H, m), 6.75−6.69 (3H, m), 5.46 (1H, t, J = 6.8 Hz), 5.07−5.00 (2H, m), 4.33 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.31 (3H, s), 2.19 (3H, s), 2.14−1.95 (8H, m), 1.79 (3H, s), 1.69 (3H, s), 1.57 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.6, 184.6, 159.1, 146.2, 143.4, 139.4, 137.6, 134.8, 133.44, 133.38, 132.3, 132.2, 131.1, 129.1, 128.7, 126.4, 126.3, 124.3, 121.5, 119.2, 115.8, 111.7, 74.0, 39.7, 39.2, 26.5, 26.4, 26.1, 21.6,

16.5, 16.1, 14.0, 12.8. HRMS ([M + Na]+) m/z calcd for C33H38NaO3 505.2719; found 505.2722. 2-Methyl-3-((2E,6E,10E)-3,7,11-trimethyl-12-(4nitrophenoxy)dodeca-2,6,10-trien-1-yl)naphthalene-1,4-dione (18). Similar to the synthesis of 10 from 21, the crude product 18, which was obtained from the mixture of 22 (46 mg, 117 μmol), pnitrophenol (49 mg, 351 μmol), and triphenylphosphine (92 mg, 351 μmol) in THF (4 mL) and diisopropyl azodicarboxylate (71 mg, 351 μmol) in THF (1.5 mL), was purified by silica gel column chromatography (n-hexane/ethyl acetate = 10:1), giving 18 (38 mg, 63%) as a yellow oil. 1H NMR (400 MHz, CDCl3): δ 8.18−8.15 (2H, m), 8.09−8.06 (2H, m), 7.70−7.68 (2H, m), 6.96−6.93 (2H, m), 5.51−5.48 (1H, m), 5.07−5.00 (2H, m), 4.45 (2H, s), 3.37 (2H, d, J = 6.8 Hz), 2.18 (3H, s), 2.16−1.96 (8H, m), 1.79 (3H, s), 1.69 (3H, s), 1.57 (3H, s). 13C NMR (100 MHz, CDCl3): δ 185.5, 184.6, 164.1, 146.2, 143.4, 141.4, 137.4, 134.5, 133.44, 133.39, 132.24, 132.21, 130.0, 129.8, 126.4, 126.3, 125.9, 124.5, 119.3, 114.8, 74.8, 39.7, 39.0, 26.5, 26.3, 26.1, 16.5, 16.0, 13.8, 12.8. HRMS ([M + H]+) m/z calcd for C32H36NO5 514.2593; found 514.2591. Ethics Statement. All animal experimental protocols were performed in accordance with the Guidelines for Animal Experiments at Shibaura Institute of Technology and were approved by the Animal Research and Ethics Committee of Shibaura Institute of Technology, Saitama, Japan. All surgical procedures were performed under sodium pentobarbital anesthesia, and all efforts were made to minimize suffering. Isolation of Mouse Embryonic Cerebral-Derived Neural Stem Cells. C57BL/6J female mice at 14 days of pregnancy were sacrificed by cervical dislocation, the uterus was taken out, and fetuses were removed from the uterus. The fetuses were decapitated, the scalp and parietal bone were stripped in L-15 medium, and the cerebrum was removed. Under stereoscopic microscope observation, the meninges and blood were completely removed and the cerebrum was washed 5 times with L-15 medium. To 9 mL of L-15 medium was added 1 mL of 2.5 g/L trypsin solution and 100 μL of DNase I solution, and the cerebrum was added and gently stirred at 37 °C for 20−25 min. DMEM (low glucose) medium containing 10% FCS was added to the trypsin and DNase I-treated cerebrum, the cerebrum was loosened by pipetting, and the cells were dispersed and centrifuged. The supernatant was discarded. DMEM (low glucose) containing 10% FCS medium was added to loosen the cells and then centrifuged. After this operation was again performed, the cells were suspended in LDMEM medium containing 10% FCS. A plate-coated glass bottom culture dish was seeded at 3 × 106 cells/dish and cultured at 37 °C for 1 day in the presence of 5% CO2. Evaluation of Cerebral Nerve Cell Differentiation by Immunostaining. The medium was removed from the isolated neural stem cells and replaced with 10% FCS containing DMEM (low glucose) medium supplemented with vitamin K derivative to 10−6 M. For control samples, ethanol was used so that the ethanol content in the medium was 0.1%. The cells were cultured for 4 days while changing the medium every 2 days at 37 °C in the presence of 5% CO2. The medium was removed, the cells were washed with PBS(−), PBS(−) containing 4% paraformaldehyde was added, and the cells were allowed to stand for 20 min at room temperature to fix the cells. The cells were then washed 3 times with PBS(−), and then the cells were covered with PBS(−) containing 0.2% Triton X-100 and left at room temperature for 5 min. Then, 10% goat-serum-containing PBS anti-Map 2 antibody was added dropwise as a primary antibody and allowed to react overnight at 4 °C. After washing three times with PBS(−), CF594 dye was added dropwise as a secondary antibody, the reaction was allowed to proceed for 1 h at room temperature in a container, and washing was carried out three times with PBS(−), and then the same procedure was carried out using anti Gfap antibody as the primary antibody and CF488A dye as the secondary antibody. The cells were washed three times with PBS(−) and then sealed with an encapsulant containing DAPI. The spectra for DAPI (excitation wavelength 360 nm, fluorescence wavelength 460 nm), CF488A (excitation wavelength 490 nm, fluorescence wavelength 515 nm), and

13

2595

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596

Journal of Medicinal Chemistry

Brief Article

CF594 (excitation wavelength 593 nm, fluorescence wavelength 614 nm) were observed. Evaluation of Differentiation-Inducing Activity of Vitamin K Analogues. After the cells were seeded and cultured for 24 h, they were treated with 1 μM vitamin K analogues and control (ethanol) for 4 days. Then the cells were collected and their mRNA were extracted. The mRNA level of Map2, Gfap, and β-actin were quantitated with real-time PCR method. The differentiation activity of vitamin K analogues toward neuronal cells or astrocyte cells was calculated from the ratios of mRNA levels of Map2/β-actin or Gfap/β-actin. Furthermore, selective differentiation activity of vitamin K analogues toward neuronal cells was calculated from the relative ratio of the mRNA of Map2/Gfap. The data were normalized with respect to the EtOH control which was reported as 1.0. The β-actin was used for a house-keeping gene.

■

(6) Li, J.; Lin, J. C.; Wang, H.; Peterson, J. W.; Furie, B. C.; Furie, B.; Booth, S. L.; Volpe, J. J.; Rosenberg, P. A. Novel role of vitamin K in preventing oxidative injury to developing oligodendrocytes and neurons. J. Neurosci. 2003, 23, 5816−5826. (7) Suhara, Y.; Hirota, Y.; Hanada, N.; Nishina, S.; Eguchi, S.; Sakane, R.; Nakagawa, K.; Wada, A.; Takahashi, K.; Tokiwa, H.; Okano, T. Synthetic small molecules derived from natural vitamin K homologues that induce selective neuronal differentiation of neuronal progenitor cells. J. Med. Chem. 2015, 58, 7088−7092. (8) Suhara, Y.; Watanabe, M.; Motoyoshi, S.; Nakagawa, K.; Wada, A.; Takeda, K.; Takahashi, K.; Tokiwa, H.; Okano, T. Synthesis of new agonists: insights into the biological role of the side chain part of vitamin K analogues as steroid and xenobiotic receptor (SXR). J. Med. Chem. 2011, 54, 4918−4922. (9) Fujii, S.; Shimizu, A.; Takeda, N.; Oguchi, K.; Katsurai, T.; Shirakawa, H.; Komai, M.; Kagechika, H. Systematic synthesis and anti-inflammatory activity of ω-carboxylated menaquinone derivativesInvestigations on identified and putative vitamin K2 metabolites. Bioorg. Med. Chem. 2015, 23, 2344−2352. (10) Hattori, T.; Takei, N.; Mizuno, Y.; Kato, K.; Kohsaka, S. Neurotrophic and neuroprotective effects of neuron-specific enolase on cultured neurons from embryonic rat brain. Neurosci. Res. 1995, 21, 191−198. (11) Deng, S.; Hou, G.; Xue, Z.; Zhang, L.; Zhou, Y.; Liu, C.; Liu, Y.; Li, Z. Vitamin E isomer δ-tocopherol enhances the efficiency of neural stem cell differentiation via L-type calcium channel. Neurosci. Lett. 2015, 585, 166−170.

ASSOCIATED CONTENT

S Supporting Information *

The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.jmedchem.6b01717. 1 H NMR and 13C NMR spectra of 7−18; HPLC data of 7−18 used in biological assays (PDF) Molecular formula strings and some data (CSV)

■

AUTHOR INFORMATION

Corresponding Author

*Phone: +81-48-720-6043. Fax: +81-48-720-6011. E-mail: [email protected]. ORCID

Yoshihisa Hirota: 0000-0002-6462-9479 Yoshitomo Suhara: 0000-0002-4770-2910 Notes

The authors declare no competing financial interest.

■

ACKNOWLEDGMENTS Y.S. acknowledges The Naito Foundation. This study was supported in part by a Grant-in-Aid for Scientific Research KAKENHI (Grant 16K08325 to Y.S.) from the Japan Society for Promotion of Science.

■ ■

ABBREVIATIONS USED NPC, neural progenitor cell; Map2, microtubule-associated protein 2; Gfap, glial fibrillary acidic protein REFERENCES

(1) Bonner, J. F.; Haas, C. J.; Fischer, I. Preparation of neural stem cells and progenitors: neuronal production and grafting applications. Methods Mol. Biol. 2013, 1078, 65−88. (2) Jin, K.; Peel, A. L.; Mao, X. O.; Xie, L.; Cottrell, B. A.; Henshall, D. C.; Greenberg, D. A. Increased hippocampal neurogenesis in Alzheimer’s disease. Proc. Natl. Acad. Sci. U. S. A. 2004, 101, 343−347. (3) Taylor, C. J.; Jhaveri, D. J.; Bartlett, P. F. The therapeutic potential of endogenous hippocampal stem cells for the treatment of neurological disorders. Front. Cell. Neurosci. 2013, 7, 5. (4) Kakeya, H.; Takahashi, I.; Okada, G.; Isono, K.; Osada, H. Epolactaene, a novel neuritogenic compound in human neuroblastoma cells, produced by a marine fungus. J. Antibiot. 1995, 48, 733−735. (5) Okano, T.; Shimomura, Y.; Yamane, M.; Suhara, Y.; Kamao, M.; Sugiura, M.; Nakagawa, K. Conversion of phylloquinone (Vitamin K1) into menaquinone-4 (Vitamin K2) in mice: two possible routes for menaquinone-4 accumulation in cerebra of mice. J. Biol. Chem. 2008, 283, 11270−11279. 2596

DOI: 10.1021/acs.jmedchem.6b01717 J. Med. Chem. 2017, 60, 2591−2596